01 1Assia Chemical Industries Ltd.
02 1Cambrex Profarmaco Milano S. r. l.
03 1Daiwa Pharmaceutical Industries Co., Ltd.
04 2Hetero Labs Limited
05 1Polaris AI Pharma Corp.
06 1Topharman Shandong Co. ,Ltd
07 1Yoshindo Co., Ltd.
25
PharmaCompass offers a list of Aripiprazole API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Aripiprazole manufacturer or Aripiprazole supplier for your needs.
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A CAS-129722-12-9 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-129722-12-9, including repackagers and relabelers. The FDA regulates CAS-129722-12-9 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-129722-12-9 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A CAS-129722-12-9 supplier is an individual or a company that provides CAS-129722-12-9 active pharmaceutical ingredient (API) or CAS-129722-12-9 finished formulations upon request. The CAS-129722-12-9 suppliers may include CAS-129722-12-9 API manufacturers, exporters, distributors and traders.
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The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The CAS-129722-12-9 Drug Master File in Japan (CAS-129722-12-9 JDMF) empowers CAS-129722-12-9 API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the CAS-129722-12-9 JDMF during the approval evaluation for pharmaceutical products. At the time of CAS-129722-12-9 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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